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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 37974 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepCAMBIA 1300
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Backbone manufacturerCambia Labs
- Backbone size w/o insert (bp) 8917
- Total vector size (bp) 12400
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Modifications to backboneCLCrV VIGS B component 1.3 mer was inserted between the SacI and HindIII sites in the pCAMBIA 1300 backbone.
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Vector typeAgrobacterium Binary
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Selectable markersHygromycin
Growth in Bacteria
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Bacterial Resistance(s)Kanamycin, 50 μg/mL
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Growth Temperature37°C
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Growth Strain(s)NEB Stable
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert namepJRTCLCrVB1.3
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Alt nameJRTB1.3
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Alt nameCLCrVB1.3
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SpeciesBegomovirus
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Insert Size (bp)3483
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site SacI (not destroyed)
- 3′ cloning site HindIII (not destroyed)
- 5′ sequencing primer AACAGCTATGACCATG
- 3′ sequencing primer GTAAAACGACGGCCAGT (Common Sequencing Primers)
Resource Information
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Article Citing this Plasmid
Terms and Licenses
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Academic/Nonprofit Terms
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Industry Terms
- Not Available to Industry
Trademarks:
- Zeocin® is an InvivoGen trademark.
Depositor Comments
Addgene NGS results have detected an IS5 family transposase upstream of the kanamycin resistance cassette. This element had no effect on virus-induced gene silencing of genes in cotton in the depositing lab. However, the concentration of kanamycin for selection may need to be reduced from 50 to 25 mg/l.
These plasmids were created by your colleagues. Please acknowledge the Principal Investigator, cite the article in which the plasmids were described, and include Addgene in the Materials and Methods of your future publications.
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For your Materials & Methods section:
pJRT.Agro.CLCrVB1.3 was a gift from Niki Robertson (Addgene plasmid # 37974 ; http://n2t.net/addgene:37974 ; RRID:Addgene_37974) -
For your References section:
Method: low-cost delivery of the cotton leaf crumple virus-induced gene silencing system. Tuttle JR, Haigler CH, Robertson D. Plant Methods. 2012 Aug 1;8(1):27. doi: 10.1186/1746-4811-8-27. 10.1186/1746-4811-8-27 PubMed 22853641